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Widespread state-dependent shifts in cerebellar activity in locomoting mice

Author(s): Ozden, Ilker; Dombeck, Daniel; Hoogland, Tycho; Tank, David; Wang, Samuel

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Abstract: Excitatory drive enters the cerebellum via mossy fibers, which activate granule cells, and climbing fibers, which activate Purkinje cell dendrites. Until now, the coordinated regulation of these pathways has gone unmonitored in spatially resolved neuronal ensembles, especially in awake animals. We imaged cerebellar activity using functional two-photon microscopy and extracellular recording in awake mice locomoting on an air-cushioned spherical treadmill. We recorded from putative granule cells, molecular layer interneurons, and Purkinje cell dendrites in zone A of lobule IV/V, representing sensation and movement from trunk and limbs. Locomotion was associated with widespread increased activity in granule cells and interneurons, consistent with an increase in mossy fiber drive. At the same time, dendrites of different Purkinje cells showed increased co-activation, reflecting increased synchrony of climbing fiber activity. In resting animals, aversive stimuli triggered increased activity in granule cells and interneurons, as well as increased Purkinje cell co-activation that was strongest for neighboring dendrites and decreased smoothly as a function of mediolateral distance. In contrast with anesthetized recordings, no 1-10 Hz oscillations in climbing fiber activity were evident. Once locomotion began, responses to external stimuli in all three cell types were strongly suppressed. Thus climbing and mossy fiber representations can shift together within a fraction of a second, reflecting in turn either movement-associated activity or external stimuli.
Publication Date: 3-Aug-2012
Citation: Ozden, Ilker, Dombeck, Daniel A, Hoogland, Tycho M, Tank, David W, Wang, Samuel S-H. (Widespread state-dependent shifts in cerebellar activity in locomoting mice. PLoS One, 7 e42650 - e42650. doi:10.1371/journal.pone.0042650
DOI: doi:10.1371/journal.pone.0042650
ISSN: 1932-6203
Pages: e42650 - e42650
Type of Material: Journal Article
Journal/Proceeding Title: PLoS One
Version: Final published version. This is an open access article.

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